Ikeda, Yoshitsugu published the artcileReactions of acyl peroxides. I. The photochemical decomposition of benzoyl peroxide in glacial acetic acid, Application In Synthesis of 13312-84-0, the publication is Nippon Kagaku Zasshi (1958), 354-8, database is CAplus.
Bz2O2 (I) (24.2 g.) in 1 l. HOAc was irradiated by light (2537 A.) 50 hrs. at 20°. At the end of this period, unreacted I was less than 0.5 g., and CO2, which was removed and absorbed in KOH as it was evolved, was 1.85 g. from 2 runs. Fractional distillation gave 5 g. C6H6. (CH2CO2H)2 (2.3 g.) was first obtained from the residue and steam distillation yielded 9.1 g. BzOH and 15.9 g. neutral substance (II). The residue from the steam distillation gave 1.1 g. neutral substance (III), 1.2 g. homophthalic acid (IV), 0.9 g. homoisophthalic acid (V), 1.5 g. homoterephthalic acid (VI), 2.3 g. p-PhC6H4CO2H (VII), and 5.1 g. resinous material. II and III gave 3.8 g. Ph2, 2.2 g. BzOH, and 1.8 g. PhOH. Thus II and III were mixtures of Ph2 and BzOPh. Thermal decomposition of I was neglected because the rate was too small. The products were related as follows. I decomposed to BzO• (VIII). VIII decomposed to Ph• and CO2 and with AcOH produced BzOH and •CH2CO2H (IX). Ph• also reacted with AcOH to produce C6H6 and IX. IX combined to produce (CH2CO2H)2 and reacted with BzOH to give VI. VIII and IX gave IV, V, and VI, which were also produced from I and IX. The formation of BzOPh and Ph2 was attributed to induced decomposition of I and to the recombination of VIII and Ph• or Ph• itself because of the accumulation at rather low temperature
Nippon Kagaku Zasshi published new progress about 13312-84-0. 13312-84-0 belongs to nitriles-buliding-blocks, auxiliary class Chloride,Nitrile,Benzene,Alcohol,Benzene Compounds, name is 2-(2-Chlorophenyl)-2-hydroxyacetonitrile, and the molecular formula is C8H6ClNO, Application In Synthesis of 13312-84-0.
Referemce:
https://en.wikipedia.org/wiki/Nitrile,
Nitriles – Chemistry LibreTexts